Regulation of VEGFA, KRAS, and NFE2L2 Oncogenes by MicroRNAs in Head and Neck Cancer

Detalhes bibliográficos
Autor(a) principal: Cuzziol, Caroline Izak
Data de Publicação: 2022
Outros Autores: Marzochi, Ludimila Leite, Possebon, Vitória Scavacini [UNESP], Kawasaki-Oyama, Rosa Sayoko, Mattos, Marlon Fraga, Junior, Vilson Serafim [UNESP], Ferreira, Letícia Antunes Muniz, Pavarino, Érika Cristina, Castanhole-Nunes, Márcia Maria Urbanin, Goloni-Bertollo, Eny Maria
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.3390/ijms23137483
http://hdl.handle.net/11449/241676
Resumo: Mutations and alterations in the expression of VEGFA, KRAS, and NFE2L2 oncogenes play a key role in cancer initiation and progression. These genes are enrolled not only in cell proliferation control, but also in angiogenesis, drug resistance, metastasis, and survival of tumor cells. MicroRNAs (miRNAs) are small, non-coding regulatory RNA molecules that can regulate post-transcriptional expression of multiple target genes. We aimed to investigate if miRNAs hsa-miR-17-5p, hsa-miR-1405p, and hsa-miR-874-3p could interfere in VEGFA, KRAS, and NFE2L2 expression in cell lines derived from head and neck cancer (HNC). FADU (pharyngeal cancer) and HN13 (oral cavity cancer) cell lines were transfected with miR-17-5p, miR-140-5p, and miR-874-3p microRNA mimics. RNA and protein expression analyses revealed that miR-17-5p, miR-140-5p and miR-874-3p overexpression led to a downregulation of VEGFA, KRAS, and NFE2L2 gene expression in both cell lines analyzed. Taken together, our results provide evidence for the establishment of new biomarkers in the diagnosis and treatment of HNC.
id UNSP_3e9591f654b464038f1418a5bf1e92b1
oai_identifier_str oai:repositorio.unesp.br:11449/241676
network_acronym_str UNSP
network_name_str Repositório Institucional da UNESP
repository_id_str 2946
spelling Regulation of VEGFA, KRAS, and NFE2L2 Oncogenes by MicroRNAs in Head and Neck CancerangiogenesismiR-140-5pmiR-17-5pmiR-874-3pMutations and alterations in the expression of VEGFA, KRAS, and NFE2L2 oncogenes play a key role in cancer initiation and progression. These genes are enrolled not only in cell proliferation control, but also in angiogenesis, drug resistance, metastasis, and survival of tumor cells. MicroRNAs (miRNAs) are small, non-coding regulatory RNA molecules that can regulate post-transcriptional expression of multiple target genes. We aimed to investigate if miRNAs hsa-miR-17-5p, hsa-miR-1405p, and hsa-miR-874-3p could interfere in VEGFA, KRAS, and NFE2L2 expression in cell lines derived from head and neck cancer (HNC). FADU (pharyngeal cancer) and HN13 (oral cavity cancer) cell lines were transfected with miR-17-5p, miR-140-5p, and miR-874-3p microRNA mimics. RNA and protein expression analyses revealed that miR-17-5p, miR-140-5p and miR-874-3p overexpression led to a downregulation of VEGFA, KRAS, and NFE2L2 gene expression in both cell lines analyzed. Taken together, our results provide evidence for the establishment of new biomarkers in the diagnosis and treatment of HNC.Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Research Unit of Genetics and Molecular Biology (UPGEM) Department of Molecular Biology Faculty of Medicine of Sao Jose do Rio Preto (FAMERP)Institute of Biosciences Humanities and Exact Sciences São Paulo State University (Unesp), Campus Sao Jose do Rio PretoInstitute of Biosciences Humanities and Exact Sciences São Paulo State University (Unesp), Campus Sao Jose do Rio PretoFAPESP: 2015/04403-8FAPESP: 2018/26166-6FAPESP: 2020/03209-1CNPq: 310987/2018-0Faculty of Medicine of Sao Jose do Rio Preto (FAMERP)Universidade Estadual Paulista (UNESP)Cuzziol, Caroline IzakMarzochi, Ludimila LeitePossebon, Vitória Scavacini [UNESP]Kawasaki-Oyama, Rosa SayokoMattos, Marlon FragaJunior, Vilson Serafim [UNESP]Ferreira, Letícia Antunes MunizPavarino, Érika CristinaCastanhole-Nunes, Márcia Maria UrbaninGoloni-Bertollo, Eny Maria2023-03-01T21:16:21Z2023-03-01T21:16:21Z2022-07-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://dx.doi.org/10.3390/ijms23137483International Journal of Molecular Sciences, v. 23, n. 13, 2022.1422-00671661-6596http://hdl.handle.net/11449/24167610.3390/ijms231374832-s2.0-85133368928Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengInternational Journal of Molecular Sciencesinfo:eu-repo/semantics/openAccess2023-03-01T21:16:21Zoai:repositorio.unesp.br:11449/241676Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T19:46:50.015774Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Regulation of VEGFA, KRAS, and NFE2L2 Oncogenes by MicroRNAs in Head and Neck Cancer
title Regulation of VEGFA, KRAS, and NFE2L2 Oncogenes by MicroRNAs in Head and Neck Cancer
spellingShingle Regulation of VEGFA, KRAS, and NFE2L2 Oncogenes by MicroRNAs in Head and Neck Cancer
Cuzziol, Caroline Izak
angiogenesis
miR-140-5p
miR-17-5p
miR-874-3p
title_short Regulation of VEGFA, KRAS, and NFE2L2 Oncogenes by MicroRNAs in Head and Neck Cancer
title_full Regulation of VEGFA, KRAS, and NFE2L2 Oncogenes by MicroRNAs in Head and Neck Cancer
title_fullStr Regulation of VEGFA, KRAS, and NFE2L2 Oncogenes by MicroRNAs in Head and Neck Cancer
title_full_unstemmed Regulation of VEGFA, KRAS, and NFE2L2 Oncogenes by MicroRNAs in Head and Neck Cancer
title_sort Regulation of VEGFA, KRAS, and NFE2L2 Oncogenes by MicroRNAs in Head and Neck Cancer
author Cuzziol, Caroline Izak
author_facet Cuzziol, Caroline Izak
Marzochi, Ludimila Leite
Possebon, Vitória Scavacini [UNESP]
Kawasaki-Oyama, Rosa Sayoko
Mattos, Marlon Fraga
Junior, Vilson Serafim [UNESP]
Ferreira, Letícia Antunes Muniz
Pavarino, Érika Cristina
Castanhole-Nunes, Márcia Maria Urbanin
Goloni-Bertollo, Eny Maria
author_role author
author2 Marzochi, Ludimila Leite
Possebon, Vitória Scavacini [UNESP]
Kawasaki-Oyama, Rosa Sayoko
Mattos, Marlon Fraga
Junior, Vilson Serafim [UNESP]
Ferreira, Letícia Antunes Muniz
Pavarino, Érika Cristina
Castanhole-Nunes, Márcia Maria Urbanin
Goloni-Bertollo, Eny Maria
author2_role author
author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Faculty of Medicine of Sao Jose do Rio Preto (FAMERP)
Universidade Estadual Paulista (UNESP)
dc.contributor.author.fl_str_mv Cuzziol, Caroline Izak
Marzochi, Ludimila Leite
Possebon, Vitória Scavacini [UNESP]
Kawasaki-Oyama, Rosa Sayoko
Mattos, Marlon Fraga
Junior, Vilson Serafim [UNESP]
Ferreira, Letícia Antunes Muniz
Pavarino, Érika Cristina
Castanhole-Nunes, Márcia Maria Urbanin
Goloni-Bertollo, Eny Maria
dc.subject.por.fl_str_mv angiogenesis
miR-140-5p
miR-17-5p
miR-874-3p
topic angiogenesis
miR-140-5p
miR-17-5p
miR-874-3p
description Mutations and alterations in the expression of VEGFA, KRAS, and NFE2L2 oncogenes play a key role in cancer initiation and progression. These genes are enrolled not only in cell proliferation control, but also in angiogenesis, drug resistance, metastasis, and survival of tumor cells. MicroRNAs (miRNAs) are small, non-coding regulatory RNA molecules that can regulate post-transcriptional expression of multiple target genes. We aimed to investigate if miRNAs hsa-miR-17-5p, hsa-miR-1405p, and hsa-miR-874-3p could interfere in VEGFA, KRAS, and NFE2L2 expression in cell lines derived from head and neck cancer (HNC). FADU (pharyngeal cancer) and HN13 (oral cavity cancer) cell lines were transfected with miR-17-5p, miR-140-5p, and miR-874-3p microRNA mimics. RNA and protein expression analyses revealed that miR-17-5p, miR-140-5p and miR-874-3p overexpression led to a downregulation of VEGFA, KRAS, and NFE2L2 gene expression in both cell lines analyzed. Taken together, our results provide evidence for the establishment of new biomarkers in the diagnosis and treatment of HNC.
publishDate 2022
dc.date.none.fl_str_mv 2022-07-01
2023-03-01T21:16:21Z
2023-03-01T21:16:21Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.3390/ijms23137483
International Journal of Molecular Sciences, v. 23, n. 13, 2022.
1422-0067
1661-6596
http://hdl.handle.net/11449/241676
10.3390/ijms23137483
2-s2.0-85133368928
url http://dx.doi.org/10.3390/ijms23137483
http://hdl.handle.net/11449/241676
identifier_str_mv International Journal of Molecular Sciences, v. 23, n. 13, 2022.
1422-0067
1661-6596
10.3390/ijms23137483
2-s2.0-85133368928
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv International Journal of Molecular Sciences
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.source.none.fl_str_mv Scopus
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv
_version_ 1808129118036819968